Mechanochemistry Unveiled: Non-Covalent Interactions, Cocrystals, and Polymorphism in Cyclorhodation Reactions

ABSTRACT: Systematic investigations into the mechanochemical metal-catalyzed functionalization of C–H bonds have showcased its efficacy in chemical synthesis, surpassing traditional solution-based protocols.[1] Despite this progress, the mechanistic details underlying C–H bond activation in mechanoc...

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Autores:
Hernández Barajas, José Gregorio
Tipo de recurso:
http://purl.org/coar/resource_type/c_5794
Fecha de publicación:
2024
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/41010
Acceso en línea:
https://hdl.handle.net/10495/41010
Palabra clave:
Química mecánica
Mechanical chemistry
Rodio
Rhodium
http://id.loc.gov/authorities/subjects/sh85082752
https://id.nlm.nih.gov/mesh/D012238
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-sa/2.5/co/
Description
Summary:ABSTRACT: Systematic investigations into the mechanochemical metal-catalyzed functionalization of C–H bonds have showcased its efficacy in chemical synthesis, surpassing traditional solution-based protocols.[1] Despite this progress, the mechanistic details underlying C–H bond activation in mechanochemical conditions remain poorly understood. This presentation delves into the mechanochemical synthesis of rhodacycles via ball milling of N-substrates and [Cp*RhCl2]2 in the presence of NaOAc. Notably, our study unveils through ex-situ and in-situ instrumental analyses the formation and polymorphic transformation of cocrystal intermediates between substrates and the rhodium dimer preceding the C–H activation step.[2] Furthermore, computational investigations have elucidated the stability and reactivity of these cocrystals towards acetate ion-mediated reactions. [3-4] By shedding light on these mechanistic nuances, our research advances the understanding and potential applications of mechanochemical C–H activation processes. REFERENCES  [1] S. Ni, M. Hribersek, S. K. Baddigam, F. J. L. Ingner, A. Orthaber, P. J. Gates, L. T. Pilarski, Angew. Chem. Int. Ed. 2021, 60, 6660–6666. [2] K. J. Ardila-Fierro, M. Rubčić, J. G. Hernández, Chem. Eur. J. 2022, 28, e202200737  [3] J. G. Hernández, K. J. Ardila-Fierro, S. Gómez, T. Stolar, M. Rubčić, E. Topić, C. Z. Hadad, A. Restrepo, Chem. Eur. J. 2023, 29, e202301290  [4] S. Gómez, S. Gómez, N. Rojas-Valencia, J. G. Hernández, K. J. Ardila-Fierro, T. Gómez, C. Cárdenas, C. Hadad, C. Capelli, A. Restrepo. Phys. Chem. Chem. Phys. 2024, 26, 2228.